Cas 118999-61-4,(S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphanyloxy)-propionic acid benzyl ester

118999-61-4

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Basic information

Product Name: (S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphanyloxy)-propionic acid benzyl ester
Synonyms: (S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphanyloxy)-propionic acid benzyl ester
CAS NO:118999-61-4
Molecular Formula:
Molecular Weight: 721.915
EINECS: N/A
Product Categories: N/A
Mol File: 118999-61-4.mol
Article Data: 1

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphanyloxy)-propionic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphanyloxy)-propionic acid benzyl ester(118999-61-4)
EPA Substance Registry System: (S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphanyloxy)-propionic acid benzyl ester(118999-61-4)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 118999-61-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118999-61-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,9,9 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118999-61:
(8*1)+(7*1)+(6*8)+(5*9)+(4*9)+(3*9)+(2*6)+(1*1)=184
184 % 10 = 4
So 118999-61-4 is a valid CAS Registry Number.

118999-61-4Upstream product

118999-61-4Downstream Products

119021-51-1 (S)-2-Benzyloxycarbonylamino-3-(octadecyloxy-phenoxy-phosphoryloxy)-propionic acid benzyl ester

118999-61-4Relevant articles and documents

A GENERAL PROTOCOL FOR THE PREPARATION OF PHOSPHOLIPIDS VIA PHOSPHITE COUPLING

Martin, Stephen F.,Josey, John A.

, p. 3631 - 3634 (2007/10/02)

A method for the facile preparation of a variety of phospholipids and their derivatives has been developed that utilizes a highly efficient phosphite coupling procedure for the synthesis of a phosphite triester, which may then be readily transformed into the corresponding phosphate diester by sequential oxidation and O-deprotection.

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